Abstract
A six months old female infant was found multiple anomalies and repeatedly admitted to our hospital after birth. Esophageal atresia with distal tracheo-esophageal fistula and duodenal atresia was diagnosed by X-ray and completely surgically repaired. Echocardiography showed truncus arteriosus type Al with persistent ductus arteriosus. The hemodynamic status was temporally stabilized by B-T shunt creation. She had recurrent urinary tract infection. The renal echo showed severe right hydronephrosis and right ureter dilatation at birth which spontaneous regressed after subsequent follow-up. The VCUG showed that the urethral meatos located at anterior vaginal wall. We will present and discuss this rare urogenital condition- female hypospadia with VATER association.
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Lin, J., Chen, C., Lai, J. et al. VATER association with female hypospadia. Genet Med 1, 58 (1999). https://doi.org/10.1097/00125817-199901000-00068
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DOI: https://doi.org/10.1097/00125817-199901000-00068